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Completed Observational

Retrospective Study to Assess the Evolution of MRI or CT Lesions in Treated CNS Nocardiosis

NCT07013006 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-09-25
Last updated
2026-10-27

Condition(s) studied

Nocardiosis

Investigational drug(s) / intervention(s)

Collection of data from the patient's medical file

Collection of data from the patient's medical file: Collection of data from the patient's medical file.

Study summary

Nocardiosis is a rare infection caused by bacteria of the genus Nocardia spp. It primarily affects immunocompromised individuals, such as solid organ or hematopoietic stem cell transplant recipients, as well as individuals with anti-GM-CSF antibodies. The infection typically begins by inhalation, affecting the lungs, with frequent hematogenous spread to the brain and soft tissues. Cerebral involvement is present in 20 to 40% of cases, although 40% of patients remain neurologically asymptomatic.

Treatment consists of prolonged antibiotic therapy and, sometimes, surgical drainage for large or refractory abscesses. Mortality associated with cerebral involvement varies between 20 and 40%. Although radiological improvements are observed under treatment, the link between image changes and clinical prognosis remains uncertain. Regular radiological monitoring is recommended during and after treatment, although the expected evolution has not been described in the literature.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Minor or adult patient with cerebral nocardiosis, defined by the presence of compatible clinical and radiological signs associated with the detection of Nocardia spp. in a biological sample (cerebral or extracerebral). * With available imaging tests: * All patients with 3 brain imaging tests at the 3 stages of treatment: within 2 weeks of diagnosis, upon transition to maintenance treatment (3-6 weeks after the start of treatment), and at the end of treatment (between 1 month before and 1 month after the end of antibiotic treatment). MRI scans are preferred; in the absence of MRI images, contrast-enhanced CT scans will be included. * OR: any patient who has undergone an MRI and a contrast-enhanced CT scan within two weeks of diagnosis, with the two tests performed within 72 hours of each other. * OR: any patient with a multimodal brain MRI at any time during infection, preferably within one month of diagnosis. Exclusion Criteria: * Refusal or impossibility of information.

Primary outcome measure(s)

  • Percentage reduction in cerebral nocardiosis lesions — 12 months
    Percentage reduction in cerebral nocardiosis lesions in patients with a favorable evolution and those with an unfavorable evolution at 12 months from diagnosis.

Trial sites (13)

FacilityCityRegionStatus
Hôpital Avicenne Bobigny France
Hôpital Ambroise-Paré Boulogne-Billancourt France
Hôpital Beaujon Clichy France
Hôpital Mondor Créteil France
Hôpital Bicêtre Le Kremlin-Bicêtre France
Hôpital Saint-Louis- Hôpital Lariboisière Paris France
Hôpital Armand-Trousseau Paris France
Hôpital Saint-Antoine Paris France
Hôpital Pitié-Salpêtrière Paris France
Hôpital Cochin Paris France
Hôpital Européen Georges-Pompidou, HEGP Paris France
Hôpital Necker-Enfants Malades Paris France
Hôpital Bichat - Claude-Bernard Paris France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07013006 on ClinicalTrials.gov ↗ ← All trials in France